RecruitingNCT04635111

A Long-term Study Evaluating Hepatotoxicity Associated With TURALIO™ (Pexidartinib) Treatment

A Long-term Study to Further Evaluate the Risk of Hepatotoxicity Associated With TURALIO™ (Pexidartinib) Treatment


Sponsor

Daiichi Sankyo

Enrollment

30 participants

Start Date

Jan 7, 2021

Study Type

OBSERVATIONAL

Conditions

Summary

A study to evaluate the long-term risk of hepatic failure with TURALIO™ (pexidartinib) and the mechanism of liver injury based upon optional liver biopsy information among patients who received or are receiving TURALIO™ (pexidartinib) and experience hepatotoxicity.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called TURALIO™ for people with hepatotoxicity and tenosynovial giant cell tumor. The study is currently recruiting participants at 8 locations. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGTURALIO™

This is a non-interventional, observational study to evaluate long-term risk of hepatic failure associated with TURALIO™ (pexidartinib) treatment. No study medication will be provided to the participants.


Locations(8)

Kamalesh K Sankhala MD INC

Santa Monica, California, United States

Sarcoma Oncology Research Center LLC

Santa Monica, California, United States

UCLA Hematology and Oncology

Santa Monica, California, United States

The Oncology Institute of Hope and Innovation

Whittier, California, United States

Dana-Farber Cancer Institute

Boston, Massachusetts, United States

Montefiore Medical Center

New York, New York, United States

OSU - James Comprehensive Cancer Center

Columbus, Ohio, United States

Kelsey Seybold Clinic - Pearland

Houston, Texas, United States

View Full Details on ClinicalTrials.gov

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NCT04635111


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